Agency Information Collection Activities: Proposed Collection; Comment Request, 12944-12946 [2021-04502]
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Federal Register / Vol. 86, No. 42 / Friday, March 5, 2021 / Notices
FEDERAL COMMUNICATIONS
COMMISSION
[OMB 3060–0751; FRS 17533]
Information Collection Being Reviewed
by the Federal Communications
Commission Under Delegated
Authority
Federal Communications
Commission.
ACTION: Notice and request for
comments.
AGENCY:
As part of its continuing effort
to reduce paperwork burdens, and as
required by the Paperwork Reduction
Act of 1995 (PRA), the Federal
Communications Commission (FCC or
Commission) invites the general public
and other Federal agencies to take this
opportunity to comment on the
following information collections.
Comments are requested concerning:
whether the proposed collection of
information is necessary for the proper
performance of the functions of the
Commission, including whether the
information shall have practical utility;
the accuracy of the Commission’s
burden estimate; ways to enhance the
quality, utility, and clarity of the
information collected; ways to minimize
the burden of the collection of
information on the respondents,
including the use of automated
collection techniques or other forms of
information technology; and ways to
further reduce the information
collection burden on small business
concerns with fewer than 25 employees.
The FCC may not conduct or sponsor
a collection of information unless it
displays a currently valid Office of
Management and Budget (OMB) control
number. No person shall be subject to
any penalty for failing to comply with
a collection of information subject to the
PRA that does not display a valid OMB
control number.
DATES: Written PRA comments should
be submitted on or before May 4, 2021.
If you anticipate that you will be
submitting comments but find it
difficult to do so within the period of
time allowed by this notice, you should
advise the contact listed below as soon
as possible.
ADDRESSES: Direct all PRA comments to
Cathy Williams, FCC, via email to PRA@
fcc.gov and to Cathy.Williams@fcc.gov.
FOR FURTHER INFORMATION CONTACT: For
additional information about the
information collection, contact Cathy
Williams at (202) 418–2918.
SUPPLEMENTARY INFORMATION:
OMB Control No.: 3060–0751.
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SUMMARY:
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Title: Contracts and Concessions, 47
CFR 43.51.
Form No.: N/A.
Type of Review: Extension of a
currently approved collection.
Respondents: Business or other forprofit entities.
Number of Respondents/Responses:
20 respondents, 20 responses.
Estimated Time per Response: 6–8
hours.
Frequency of Response: On occasion
reporting requirement.
Obligation to Respond: Required to
obtain or retain benefits. The statutory
authority for this information collection
is contained in 47 U.S.C. 154, 211, 219
and 220.
Total Annual Burden: 140 hours.
Annual Cost Burden: No cost.
Privacy Act Impact Assessment: No
impact(s).
Nature and Extent of Confidentiality:
In general, there is no need for
confidentiality with this collection of
information.
Needs and Uses: This collection will
be submitted as an extension (no change
in reporting or recordkeeping
requirements) after this 60-day comment
period to the Office of Management and
Budget (OMB) in order to obtain the full
three-year clearance.
The Commission has determined that
the authorized resale of international
private lines inter-connected to the U.S.
public switched network would tend to
divert international message telephone
service (IMTS) traffic from the
settlements process and increase the
U.S. net settlements deficit. The
information will be used by the
Commission in reviewing the impact, if
any, that end-user private line
interconnections have on the
Commission’s international settlements
policy. The data will also enhance the
ability of both the Commission and
interested parties to monitor the
unauthorized resale of international
private lines that are interconnected to
the U.S. public switched network.
Federal Communications Commission.
Marlene Dortch,
Secretary.
[FR Doc. 2021–04616 Filed 3–4–21; 8:45 am]
BILLING CODE 6712–01–P
FEDERAL RESERVE SYSTEM
Formations of, Acquisitions by, and
Mergers of Bank Holding Companies
The companies listed in this notice
have applied to the Board for approval,
pursuant to the Bank Holding Company
Act of 1956 (12 U.S.C. 1841 et seq.)
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(BHC Act), Regulation Y (12 CFR part
225), and all other applicable statutes
and regulations to become a bank
holding company and/or to acquire the
assets or the ownership of, control of, or
the power to vote shares of a bank or
bank holding company and all of the
banks and nonbanking companies
owned by the bank holding company,
including the companies listed below.
The public portions of the
applications listed below, as well as
other related filings required by the
Board, if any, are available for
immediate inspection at the Federal
Reserve Bank(s) indicated below and at
the offices of the Board of Governors.
This information may also be obtained
on an expedited basis, upon request, by
contacting the appropriate Federal
Reserve Bank and from the Board’s
Freedom of Information Office at
https://www.federalreserve.gov/foia/
request.htm. Interested persons may
express their views in writing on the
standards enumerated in the BHC Act
(12 U.S.C. 1842(c)).
Comments regarding each of these
applications must be received at the
Reserve Bank indicated or the offices of
the Board of Governors, Ann E.
Misback, Secretary of the Board, 20th
Street and Constitution Avenue NW,
Washington, DC 20551–0001, not later
than April 5, 2021.
A. Federal Reserve Bank of San
Francisco (Sebastian Astrada, Director,
Applications) 101 Market Street, San
Francisco, California 94105–1579:
1. Riverview Bancorp, Inc.,
Vancouver, Washington; to become a
bank holding company upon the
conversion of its wholly-owned
subsidiary, Riverview Community Bank,
Vancouver, Washington, from a federal
savings bank to a Washington statechartered non-member bank.
Board of Governors of the Federal Reserve
System, March 2, 2021.
Michele Taylor Fennell,
Deputy Associate Secretary of the Board.
[FR Doc. 2021–04638 Filed 3–4–21; 8:45 am]
BILLING CODE P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Agency for Healthcare Research and
Quality
Agency Information Collection
Activities: Proposed Collection;
Comment Request
Agency for Healthcare Research
and Quality, HHS.
ACTION: Notice.
AGENCY:
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Federal Register / Vol. 86, No. 42 / Friday, March 5, 2021 / Notices
This notice announces the
intention of the Agency for Healthcare
Research and Quality (AHRQ) to request
that the Office of Management and
Budget (OMB) approve proposed
updates to the approved information
collection project ‘‘Safety Program in
Perinatal Care (SPPC)-II Demonstration
Project.’’
SUMMARY:
Comments on this notice must be
received by May 4, 2021.
ADDRESSES: Written comments should
be submitted to: Doris Lefkowitz,
Reports Clearance Officer, AHRQ, by
email at doris.lefkowitz@AHRQ.hhs.gov.
Copies of the proposed collection
plans, data collection instruments, and
specific details on the estimated burden
can be obtained from the AHRQ Reports
Clearance Officer.
FOR FURTHER INFORMATION CONTACT:
Doris Lefkowitz, AHRQ Reports
Clearance Officer, (301) 427–1477, or by
email at doris.lefkowitz@AHRQ.hhs.gov.
SUPPLEMENTARY INFORMATION:
DATES:
Proposed Project
Safety Program in Perinatal Care
(SPPC)-II Demonstration Project
The SPPC–II Demonstration Project
has the following goals:
(1) To implement the integrated
Alliance for Innovation on Maternal
Health (AIM)-SPPC II program in
birthing hospitals in Oklahoma and
Texas in coordination with AIM and the
respective state PQC (Perinatal Quality
Collaborative);
(2) To assess the implementation of
the integrated AIM–SPPC II program in
these hospitals; and
(3) To ascertain the short- and
medium-term impact of the integrated
AIM–SPPC II program on hospital (i.e.,
perinatal unit) teamwork and
communication, patient safety, and key
maternal health outcomes.
This study is being conducted by
AHRQ through its contractor, Johns
Hopkins University (JHU) and the AIM
program, JHU’s subcontractor, pursuant
to AHRQ’s statutory authority to
conduct and support research on
healthcare and on systems for the
delivery of such care, including
activities with respect to the quality,
effectiveness, efficiency,
appropriateness and value of healthcare
services and with respect to quality
measurement and improvement. 42
U.S.C. 299a (a)(1) and (2).
Due to continued pandemic-related
impacts on the SPPC–II study
population, we propose to update the
SPPC–II data collection by (1)
restructuring and adding questions to
the approved qualitative interview
guides to be used with AIM program
Team Leads and now frontline health
providers in the summer/fall of 2021 to
include questions to better understand
the perceived implementation context;
and (2) adding focus group discussions
in the summer/fall of 2022 to assess
perceptions of implementation and
sustainability of the SPPC–II Toolkit at
the hospital level The total burden
hours resulting from these proposed
updates to the SPPC–II data collection is
64 hours. The total estimated annual
burden hours for SPPC–II are 54,693.
Method of Collection
To achieve the goals of this project the
following updates to the data collections
will be implemented:
(a) Qualitative, semi-structured
interviews with AIM Team Leads and
frontline staff will be conducted by
phone or via zoom in the summer/fall
of 2021 to assess the perceived utility of
the training and the perceived
implementation context (including
barriers, facilitators, and strategies) in
the context of a reduced scope for
SPCC–II. In 8 hospitals, one-hour
interviews with AIM Team Leads (1 per
hospital) and 30-minute interviews with
frontline staff (4 per hospital) will be
conducted. An interview guide
developed based on the Consolidated
Framework for Implementation
Research framework will be used to
conduct the interviews, together with a
corresponding consent form. The
interview guide will be supported by
the SPPC–II tier level training specific
handouts.
(b) Focus group discussions with AIM
Team Leads and frontline staff will be
conducted by phone or via zoom in the
summer/fall of 2022 to assess
perceptions of implementation and
sustainability of the SPPC–II Toolkit at
the hospital level. We will conduct one
1-hour focus groups with AIM Team
Leads and frontline staff in each of the
8 hospitals. An interview guide
developed based on the Consolidated
Framework for Implementation
Research framework will be used to
conduct the interviews, together with a
corresponding consent form.
Estimated Annual Respondent Burden
Exhibit 1 shows only the estimated
annualized burden hours for the
respondents’ time to participate in
updates to the information collection of
the SPPC–II Demonstration Project.
One-hour qualitative interviews will
be conducted with a total of 8 AIM
Team Leads and 30-minute qualitative
interviews with 32 frontline staff in 8
hospitals. We will also conduct 8 onehour focus group discussions with a
total of 40 AIM Team Leads and
frontline staff in the same hospitals.
The total burden hours resulting from
the proposed updates to the SPPC–II
data collection is 64 hours. The total
annual burden hours are estimated to be
54,693 hours.
EXHIBIT 1—ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
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Form name
Number of
responses per
respondent
Hours per
response
Total burden
hours
Qualitative semi-structured interviews with AIM Team Leads ........................
Qualitative semi-structured interviews with frontline staff ...............................
Focus group discussions with AIM Team Leads and frontline staff ...............
8
32
40
1
1
1
1.00
0.50
1
8
16
40
Total ..........................................................................................................
80
NA
NA
64
Exhibit 2 shows only the hours and
cost of updates to the collection. The
total cost burden of the updated
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collection is estimated to be
$1,421,576.68 annually.
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Federal Register / Vol. 86, No. 42 / Friday, March 5, 2021 / Notices
EXHIBIT 2—ESTIMATED ANNUALIZED COST BURDEN
Number of
respondents
Form name
Average
hourly wage
rate *
Total burden
hours
Total cost
burden
Qualitative semi-structured interviews with AIM Team Leads ........................
Qualitative semi-structured interviews with frontline staff ...............................
Focus group discussions with AIM Team Leads and frontline staff ...............
8
32
40
8
16
40
$49.83
49.83
49.83
$398.64
797.28
1,993.20
Total ..........................................................................................................
80
64
........................
$3,189.12
* National Compensation Survey: Occupational wages in the United States May 2017 ‘‘U.S. Department of Labor, Bureau of Labor Statistics.’’
Weighted mean hourly wage for obstetrician-gynecologists ($113.10; occupation code 29–1064; 30%); nurse-midwives ($49.83; occupation code
29–1161; 30%); registered nurses ($35.36; occupation code 29–1161; 20%); and nurse practitioners ($51.86; occupation code 29–1171; 20%).
Request for Comments
In accordance with the Paperwork
Reduction Act, 44 U.S.C. 3501–3520,
comments on AHRQ’s information
collection are requested with regard to
any of the following: (a) Whether the
proposed collection of information is
necessary for the proper performance of
AHRQ’s health care research and health
care information dissemination
functions, including whether the
information will have practical utility;
(b) the accuracy of AHRQ’s estimate of
burden (including hours and costs) of
the proposed collection(s) of
information; (c) ways to enhance the
quality, utility and clarity of the
information to be collected; and (d)
ways to minimize the burden of the
collection of information upon the
respondents, including the use of
automated collection techniques or
other forms of information technology.
Comments submitted in response to
this notice will be summarized and
included in the Agency’s subsequent
request for OMB approval of the
proposed information collection. All
comments will become a matter of
public record.
scientific information submissions from
the public. Scientific information is
being solicited to inform our review on
Management of Infantile Epilepsy,
which is currently being conducted by
the AHRQ’s Evidence-based Practice
Centers (EPC) Program. Access to
published and unpublished pertinent
scientific information will improve the
quality of this review.
DATES: Submission Deadline on or
before April 5, 2021.
ADDRESSES:
Email submissions: epc@
ahrq.hhs.gov.
Print submissions:
Mailing Address: Center for Evidence
and Practice Improvement, Agency for
Healthcare Research and Quality,
ATTN: EPC SEADs Coordinator, 5600
Fishers Lane, Mail Stop 06E53A,
Rockville, MD 20857.
Shipping Address (FedEx, UPS, etc.):
Center for Evidence and Practice
Improvement, Agency for Healthcare
Research and Quality, ATTN: EPC
SEADs Coordinator, 5600 Fishers Lane,
Mail Stop 06E77D, Rockville, MD
20857.
Dated: March 1, 2021.
Marquita Cullom,
Associate Director.
Jenae Benns, Telephone: 301–427–1496
or Email: epc@ahrq.hhs.gov.
SUPPLEMENTARY INFORMATION: The
Agency for Healthcare Research and
Quality has commissioned the
Evidence-based Practice Centers (EPC)
Program to complete a review of the
evidence for Management of Infantile
Epilepsy. AHRQ is conducting this
systematic review pursuant to Section
902 of the Public Health Service Act, 42
U.S.C. 299a.
The EPC Program is dedicated to
identifying as many studies as possible
that are relevant to the questions for
each of its reviews. In order to do so, we
are supplementing the usual manual
and electronic database searches of the
literature by requesting information
from the public (e.g., details of studies
conducted). We are looking for studies
that report on Management of Infantile
Epilepsy, including those that describe
[FR Doc. 2021–04502 Filed 3–4–21; 8:45 am]
BILLING CODE 4160–90–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Agency for Healthcare Research and
Quality
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Supplemental Evidence and Data
Request on Management of Infantile
Epilepsy
Agency for Healthcare Research
and Quality (AHRQ), HHS.
ACTION: Request for Supplemental
Evidence and Data Submissions.
AGENCY:
The Agency for Healthcare
Research and Quality (AHRQ) is seeking
SUMMARY:
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FOR FURTHER INFORMATION CONTACT:
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adverse events. The entire research
protocol is available online at: https://
effectivehealthcare.ahrq.gov/products/
management-infantile-epilepsy/
research-protocol.
This is to notify the public that the
EPC Program would find the following
information on Management of Infantile
Epilepsy helpful:
D A list of completed studies that
your organization has sponsored for this
indication. In the list, please indicate
whether results are available on
ClinicalTrials.gov along with the
ClinicalTrials.gov trial number.
D For completed studies that do not
have results on ClinicalTrials.gov, a
summary, including the following
elements: Study number, study period,
design, methodology, indication and
diagnosis, proper use instructions,
inclusion and exclusion criteria,
primary and secondary outcomes,
baseline characteristics, number of
patients screened/eligible/enrolled/lost
to follow-up/withdrawn/analyzed,
effectiveness/efficacy, and safety results.
D A list of ongoing studies that your
organization has sponsored for this
indication. In the list, please provide the
ClinicalTrials.gov trial number or, if the
trial is not registered, the protocol for
the study including a study number, the
study period, design, methodology,
indication and diagnosis, proper use
instructions, inclusion and exclusion
criteria, and primary and secondary
outcomes.
D Description of whether the above
studies constitute ALL Phase II and
above clinical trials sponsored by your
organization for this indication and an
index outlining the relevant information
in each submitted file.
Your contribution is very beneficial to
the Program. Materials submitted must
be publicly available or able to be made
public. Materials that are considered
confidential; marketing materials; study
types not included in the review; or
information on indications not included
in the review cannot be used by the EPC
Program. This is a voluntary request for
information, and all costs for complying
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[Federal Register Volume 86, Number 42 (Friday, March 5, 2021)]
[Notices]
[Pages 12944-12946]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-04502]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Agency for Healthcare Research and Quality
Agency Information Collection Activities: Proposed Collection;
Comment Request
AGENCY: Agency for Healthcare Research and Quality, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
[[Page 12945]]
SUMMARY: This notice announces the intention of the Agency for
Healthcare Research and Quality (AHRQ) to request that the Office of
Management and Budget (OMB) approve proposed updates to the approved
information collection project ``Safety Program in Perinatal Care
(SPPC)-II Demonstration Project.''
DATES: Comments on this notice must be received by May 4, 2021.
ADDRESSES: Written comments should be submitted to: Doris Lefkowitz,
Reports Clearance Officer, AHRQ, by email at
[email protected].
Copies of the proposed collection plans, data collection
instruments, and specific details on the estimated burden can be
obtained from the AHRQ Reports Clearance Officer.
FOR FURTHER INFORMATION CONTACT: Doris Lefkowitz, AHRQ Reports
Clearance Officer, (301) 427-1477, or by email at
[email protected].
SUPPLEMENTARY INFORMATION:
Proposed Project
Safety Program in Perinatal Care (SPPC)-II Demonstration Project
The SPPC-II Demonstration Project has the following goals:
(1) To implement the integrated Alliance for Innovation on Maternal
Health (AIM)-SPPC II program in birthing hospitals in Oklahoma and
Texas in coordination with AIM and the respective state PQC (Perinatal
Quality Collaborative);
(2) To assess the implementation of the integrated AIM-SPPC II
program in these hospitals; and
(3) To ascertain the short- and medium-term impact of the
integrated AIM-SPPC II program on hospital (i.e., perinatal unit)
teamwork and communication, patient safety, and key maternal health
outcomes.
This study is being conducted by AHRQ through its contractor, Johns
Hopkins University (JHU) and the AIM program, JHU's subcontractor,
pursuant to AHRQ's statutory authority to conduct and support research
on healthcare and on systems for the delivery of such care, including
activities with respect to the quality, effectiveness, efficiency,
appropriateness and value of healthcare services and with respect to
quality measurement and improvement. 42 U.S.C. 299a (a)(1) and (2).
Due to continued pandemic-related impacts on the SPPC-II study
population, we propose to update the SPPC-II data collection by (1)
restructuring and adding questions to the approved qualitative
interview guides to be used with AIM program Team Leads and now
frontline health providers in the summer/fall of 2021 to include
questions to better understand the perceived implementation context;
and (2) adding focus group discussions in the summer/fall of 2022 to
assess perceptions of implementation and sustainability of the SPPC-II
Toolkit at the hospital level The total burden hours resulting from
these proposed updates to the SPPC-II data collection is 64 hours. The
total estimated annual burden hours for SPPC-II are 54,693.
Method of Collection
To achieve the goals of this project the following updates to the
data collections will be implemented:
(a) Qualitative, semi-structured interviews with AIM Team Leads and
frontline staff will be conducted by phone or via zoom in the summer/
fall of 2021 to assess the perceived utility of the training and the
perceived implementation context (including barriers, facilitators, and
strategies) in the context of a reduced scope for SPCC-II. In 8
hospitals, one-hour interviews with AIM Team Leads (1 per hospital) and
30-minute interviews with frontline staff (4 per hospital) will be
conducted. An interview guide developed based on the Consolidated
Framework for Implementation Research framework will be used to conduct
the interviews, together with a corresponding consent form. The
interview guide will be supported by the SPPC-II tier level training
specific handouts.
(b) Focus group discussions with AIM Team Leads and frontline staff
will be conducted by phone or via zoom in the summer/fall of 2022 to
assess perceptions of implementation and sustainability of the SPPC-II
Toolkit at the hospital level. We will conduct one 1-hour focus groups
with AIM Team Leads and frontline staff in each of the 8 hospitals. An
interview guide developed based on the Consolidated Framework for
Implementation Research framework will be used to conduct the
interviews, together with a corresponding consent form.
Estimated Annual Respondent Burden
Exhibit 1 shows only the estimated annualized burden hours for the
respondents' time to participate in updates to the information
collection of the SPPC-II Demonstration Project.
One-hour qualitative interviews will be conducted with a total of 8
AIM Team Leads and 30-minute qualitative interviews with 32 frontline
staff in 8 hospitals. We will also conduct 8 one-hour focus group
discussions with a total of 40 AIM Team Leads and frontline staff in
the same hospitals.
The total burden hours resulting from the proposed updates to the
SPPC-II data collection is 64 hours. The total annual burden hours are
estimated to be 54,693 hours.
Exhibit 1--Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of
Form name Number of responses per Hours per Total burden
respondents respondent response hours
----------------------------------------------------------------------------------------------------------------
Qualitative semi-structured interviews with AIM 8 1 1.00 8
Team Leads.....................................
Qualitative semi-structured interviews with 32 1 0.50 16
frontline staff................................
Focus group discussions with AIM Team Leads and 40 1 1 40
frontline staff................................
---------------------------------------------------------------
Total....................................... 80 NA NA 64
----------------------------------------------------------------------------------------------------------------
Exhibit 2 shows only the hours and cost of updates to the
collection. The total cost burden of the updated collection is
estimated to be $1,421,576.68 annually.
[[Page 12946]]
Exhibit 2--Estimated Annualized Cost Burden
----------------------------------------------------------------------------------------------------------------
Number of Total burden Average hourly Total cost
Form name respondents hours wage rate * burden
----------------------------------------------------------------------------------------------------------------
Qualitative semi-structured interviews with AIM 8 8 $49.83 $398.64
Team Leads.....................................
Qualitative semi-structured interviews with 32 16 49.83 797.28
frontline staff................................
Focus group discussions with AIM Team Leads and 40 40 49.83 1,993.20
frontline staff................................
---------------------------------------------------------------
Total....................................... 80 64 .............. $3,189.12
----------------------------------------------------------------------------------------------------------------
* National Compensation Survey: Occupational wages in the United States May 2017 ``U.S. Department of Labor,
Bureau of Labor Statistics.'' Weighted mean hourly wage for obstetrician-gynecologists ($113.10; occupation
code 29-1064; 30%); nurse-midwives ($49.83; occupation code 29-1161; 30%); registered nurses ($35.36;
occupation code 29-1161; 20%); and nurse practitioners ($51.86; occupation code 29-1171; 20%).
Request for Comments
In accordance with the Paperwork Reduction Act, 44 U.S.C. 3501-
3520, comments on AHRQ's information collection are requested with
regard to any of the following: (a) Whether the proposed collection of
information is necessary for the proper performance of AHRQ's health
care research and health care information dissemination functions,
including whether the information will have practical utility; (b) the
accuracy of AHRQ's estimate of burden (including hours and costs) of
the proposed collection(s) of information; (c) ways to enhance the
quality, utility and clarity of the information to be collected; and
(d) ways to minimize the burden of the collection of information upon
the respondents, including the use of automated collection techniques
or other forms of information technology.
Comments submitted in response to this notice will be summarized
and included in the Agency's subsequent request for OMB approval of the
proposed information collection. All comments will become a matter of
public record.
Dated: March 1, 2021.
Marquita Cullom,
Associate Director.
[FR Doc. 2021-04502 Filed 3-4-21; 8:45 am]
BILLING CODE 4160-90-P
